Bridging the immunogenicity of a tetravalent dengue vaccine (TAK-003) from children and adolescents to adults

被引:4
|
作者
LeFevre, Inge [1 ]
Bravo, Lulu [2 ]
Folschweiller, Nicolas [1 ]
Medina, Eduardo Lopez [3 ,4 ]
Moreira, Edson Duarte [5 ,6 ]
Nordio, Francesco [7 ]
Sharma, Mayuri [7 ]
Tharenos, Leslie M. [8 ]
Tricou, Vianney [1 ]
Watanaveeradej, Veerachai [9 ,10 ]
Winkle, Peter J. [11 ]
Biswal, Shibadas [7 ]
机构
[1] Takeda Pharmaceut Int AG, Vaccines Business Unit, Zurich, Switzerland
[2] Univ Philippines, Coll Med, Manila, Philippines
[3] Ctr Estudios Infectol Pediat CEIP, Cali, Colombia
[4] Clin Imbanaco, Grp Quironsalud, Cali, Colombia
[5] Assoc Obras Sociais Irma Dulce Hosp Santo Antonio, Salvador, BA, Brazil
[6] Fundacao Oswaldo Cruz, Salvador, BA, Brazil
[7] Takeda Vaccines Inc, Cambridge, MA 02139 USA
[8] Univ Illinois, Div Environm & Occupat Hlth Sci, Sch Publ Hlth, Chicago, IL USA
[9] Kasetsart Univ, Phramongkutklao Hosp, Dept Pediat, Bangkok, Thailand
[10] Kasetsart Univ, Fac Med, Bangkok, Thailand
[11] Anaheim Clin Trials, Anaheim, CA USA
关键词
PNEUMOCOCCAL CONJUGATE VACCINE; YELLOW-FEVER VACCINE; HUMAN-PAPILLOMAVIRUS; PARTICLE VACCINE; HEALTHY-CHILDREN; DOUBLE-BLIND; EFFICACY; SAFETY; ANTIBODIES; NEUTRALIZATION;
D O I
10.1038/s41541-023-00670-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunobridging is an important methodology that can be used to extrapolate vaccine efficacy estimates to populations not evaluated in clinical studies, and that has been successfully used in developing many vaccines. Dengue, caused by a mosquito-transmitted flavivirus endemic to many tropical and subtropical regions, is traditionally thought of as a pediatric disease but is now a global threat to both children and adults. We bridged immunogenicity data from a phase 3 efficacy study of a tetravalent dengue vaccine (TAK-003), performed in children and adolescents living in endemic areas, with an immunogenicity study in adults in non-endemic areas. Neutralizing antibody responses were comparable in both studies following receipt of a two-dose TAK-003 schedule (months 0 and 3). Similar immune responses were observed across exploratory assessments of additional humoral responses. These data support the potential for clinical efficacy of TAK-003 in adults.
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页数:9
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